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Transcervial Hysteroscopic for retained products of conception:Efficacy and Subsequent fertility

Transcervial Hysteroscopic for retained products of conception:Efficacy and Subsequent fertility

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900028633
Enrollment
Unknown
Registered
2019-12-29
Start date
2020-02-26
Completion date
Unknown
Last updated
2021-05-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

retained products of conception

Interventions

Case series:Nil

Sponsors

Department of Hysteroscopic Center, Fuxing Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Women aged older than 18 years, presence of retained products of conception, sign informed consent.

Exclusion criteria

Exclusion criteria: Nil

Design outcomes

Primary

MeasureTime frame
Fertility outcome;—

Countries

China

Contacts

Public ContactXue Yang

Department of Hysteroscopic Center, Fuxing Hospital, Capital Medical University

1172039685@qq.com+86 18810957056

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026